4.6 Article

cDNA cloning, expression, and enzymatic activity of a novel endogenous cellulase from the beetle Batocera horsfieldi

Journal

GENE
Volume 514, Issue 1, Pages 62-68

Publisher

ELSEVIER
DOI: 10.1016/j.gene.2012.08.044

Keywords

Batocera horsfieldi; Beetle; Cellulase; cDNA cloning; Insect; Enzymatic activity

Funding

  1. National Natural Science Foundation of China [30871829, 31072083]

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In this study, we report a novel cellulase [beta-1,4-endoglucanase (EGase), EC 3.2.1.4] cDNA (Bh-EGase II) belonging to the glycoside hydrolase family (GHF) 45 from the beetle Batocera horsfieldi. The Bh-EGase II gene spans 720 bp and consists of a single exon coding for 239 amino acid residues. Bh-EGase II showed 93.72% protein sequence identity to Ag-EGase II from the beetle Apriona germari. The GHF 45 catalytic site is conserved in Bh-EGase II. Bh-EGase II has three putative N-glycosylation sites at 56-58 (N-K-S), 99-101 (N-S-T), and 237-239 (N-Y-S), respectively. The cDNA encoding Bh-EGase II was expressed in baculovirus-infected insect BmN cells and Bombyx mori larvae. Recombinant Bh-EGase II from BmN cells and larval hemolymph had an enzymatic activity of approximately 928 U/mg. The enzymatic catalysis of recombinant Bh-EGase II showed the highest activity at 50 degrees C and pH 6.0. Crown Copyright (C) 2012 Published by Elsevier B.V. All rights reserved.

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